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African Journal of Biomedical Research
Ibadan Biomedical Communications Group
ISSN: 1119-5096
Vol. 6, Num. 2, 2003, pp. 109-110
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African Journal of Biomedical Research, Vol. 6, No. 2, May, 2003, pp. 109-110
Short communication
EFFICACY OF SOME ANTHELMINTICS USED IN PORCINE PRACTICE IN IBADAN , NIGERIA
AYOADE G. O., ADEJINMI J. O., ABIOLA J.O. AND LUCAS F.
Faculty of Veterinary Medicine, University of Ibadan
Received: September
2001
Accepted: June 2002
Code Number: md03021
ABSTRACT
Ninety three (93) pigs (crosses of Large white, Landrace, Hampshire and
Duroc) were screened for gastrointestinal worms before and after treatment
with the following drugs: Levamisole, Albendazole, Morantel citrate, Piperazine.,
thiabendazole and Ivermectin. The anthelmintic efficacy (measure as reduction
egg per gram (EPG) of faeces) observed ranged as follows: Ivermectin 100% Levamisole 89%;
Thiabendazole 78.0%; Albendazole 73.2%; Morantel citrate 78.7% and Piperazine 70.6%
Ivermectin and Albendazole cleared the Trichuris worms that were not cleared
by Morantel, Piperazine and Levamisole. A combination of good hygiene and strict
deworming programme will go a long way in eradication of pathogenic helminths
of livestock.
KEY WORDS: Anthelmintics, pigs, parasites, Ibadan .
INTRODUCTION
Soulsby (1968) reported that nematodes can colonise land, water, fresh water
and seas as well as parasitizing both plants and animals. Their life' cycles
require fertilized eggs being laid by the female worm, which are usually expected
in faeces. They later hatch into infective larvae outside the host and develop
no further until ingested by another or the same animal. Once in the gut, they
burrow through the mucosal wall where they undergo several moults before re-emerging
in the gut lumen to mature and perpetuate the life cycles (Soulsby, 1968; Blood
and Radostits 1995).
Gastrointestinal helminths are from cradle known to be of economic importance
in porcine practice and related fields with their effects ranging from poor
growth, unthrifthness, diarrhea, anaemia and death (Blood and Radostits, 1995).
Since losses of pigs to helminth parasites are enormous, it is imperative therefore
to carry our investigations on anthelmintic performance in the pig industry
to enable farmers plan their ways forward.
MATERIALS AND METHODS
Using disposable hand gloves inserted in the rectum faecal samples were collected
from 93 (ninety three) pigs. They were crosses of Large white, Landrace, Duroc
and Hampshire. Feacal samples collected were then dispatched into universal
glass bottles well labeled and filled to the brim to exclude air as much as
possible. This reduced the rate of development and hatching of the eggs of
worms. Where laboratory examination could not be carried out soon after collection,
samples were kept in the refrigerator at 4 0 C for not more than 24 hours.
The faecal samples were collected just before treatment and a week after treatment.
From each pig 3g of faeces were mixed with 30 ml of saturated solution of
common table salt (NaCl) in a small glass container and with the aid of sieve
the fibrous portion of the faeces was filtered. The eggs per gram (EPG) was
determined using a modified MCMaster method. Identification of helminths was
done using appropriate morphological criteria of worms and eggs (Soulsby, 1968).
Ninety three (93) pigs were divided into six groups and dewormed as follows:-
Group 1- Morantel Citrate Pyrantel pamoate (17 pigs)
Group 2 - Levamisole (17 pigs)
Group 3 - Piperazine (23 pigs)
Group 4 - Thiabendazole (10 pigs)
Group 5 - Albendazole (14 pigs)
Group 6 - Ivermectin (Ivomec ® 12 pigs)
The groups that still carry worms like trichuris were dewormed further using
Ivermectin and Albendazole. Banmith ® (Morantel citrate) was given orally
separately at 1 tablet 22mg/kg body weight. Albendazole was given orally at
250mg/kg body weight.
Ivermectin was given parenterally at a does of 1ml/50kg B.wt, Levamisole at
100mg/20kg B.wt and Piperazine was given orally at 110mg/kg body weight.
RESULTS
The result is presented in table 1. the drug efficacy of Ivermectin topped
the list with 100%, reducing the worm load from 250 to zero epg. Levamisole
followed with 89.4%, reducing the worm load from 136epg to 29epg. The weakest
is Piperazine with 70.6% efficacy. Ivermectin and Albendazole cleared the Trichuris
worms that were not cleared by Morantel, Piperazine and Levamisole.
Table 2 shows the effect of the anthelmintics on the specific pathogenic helminth
based on species Ascaris, Trichuris and strongyles.
Table 1: Drug performance of the anthelmintics in pigs
Drug used |
n |
Total EPG |
Efficacy % |
|
|
BD |
AD |
|
Piperazine |
23 |
391 |
115 |
70.59 |
Levamisole |
17 |
170 |
18 |
89.4 |
Morantel Citrate |
17 |
136 |
29 |
78.7 |
Albendazole |
14 |
168 |
45 |
73.2 |
Thiabendazole |
10 |
50 |
11 |
78 |
Ivermectin |
12 |
250 |
0 |
100 |
N = number of animals; BD = Before deworming;
AD = After deworming
DISCUSSION
Generally all the anthelmintics used reduced the worm load
is indicated in the faecal egg count within a week of administration. Ivermectin
had the best deworming effect (98%) while Piperazine is least effective (70.6%)
in this group. Ivermectin has an added advantage of being effective against
mites, thus treating mange. Piperazine is mainly effective against Ascaris
(Brander et
al ., 1990). Albendazole is also effective against Trichuris.
The need to monitor both infestation and efficacy of anthelmintics need not
be over emphasized. The battle against gastrointestinal worms continues. Drug
resistance must be arrested as early as detected.
Table 2: Effect of anthelmintic on specific pathogenic helminth Ascaris,
Trichuris and Stongyles.
Drug |
Helminths (%) |
|
Ascaris |
Trichuris |
Strongyles |
Piperazine |
52 |
48 |
48 |
Albendazole |
50 |
64 |
79 |
Thiabendazole |
60 |
70 |
70 |
Morantel citrate |
100 |
59 |
100 |
Levamisole |
77 |
77 |
77 |
Ivermectin |
100 |
100 |
100 |
REFERENCES
- Blood D. C and Radosites, O. M. (1995) . Veterinary Medicine.
A textbook of the diseases of cattle, sheep, pigs goats and horses 8 th edition,
published by Bailliene Tindal London pp 1016-1065.
- Brander E. C., Pugh D. M., Bywater R. J. and Jerkins J. W. (1990). Veterinary
Applied Pharmacology and Therapeuties, 5 th Edition Bailliena Lindal,
London pp 500-561.
- Dunne H. W. and Leman A. D. R. D. Glock, W. L. Mengeling, R. H. C. Penny
E. Scholl and B. Straw. (1982). Diseases of Swine 5 th Edition
Iowa State University Press, Ames , Iowa , U.S.A.
- Jacob D. E. (1981): Gastrointestinal parasites in pigs. Veterinary
Record 77(16) 461-462.
- Soulsby E. J. H. (1982). A textbook of helminths, arthropod
and protozoa of domesticated animals. 7 th edition, Balliere, Tindal
and Casell.
© Ibadan Biomedical Communications Group
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